科研之友
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摘要
Concern around the lack of monitoring of proteinaceous subvisible particulates in the 0.1-10 mu m range has been heightened (Carpenter et al., 2009, J Pharm Sci 98 1202-1205), primarily due to uncertainty around the potential immunogenicity risk from these particles This article, representing the opinions of a number of industry scientists, aims to further the discussion by developing a common understanding around the technical capabilities, limitations, as well as utility of monitoring this size range; reiterating that the link between aggregation and clinical immunogenicity has not been unequivocally established, and emphasizing that such particles are present in marketed products which remain safe and efficacious despite the lack of monitoring. Measurement of subvisible particulates in the <10 mu m size range has value as an aid in product development and characterization Limitations in measurement technologies, variability from container/closure, concentration, viscosity, history, and inherent batch heterogeneity, make these measurements unsuitable as specification for release and stability or for comparability, at the present time. Such particles constitute microgram levels of protein with currently monitored sizes >= 10 mu m representing the largest fraction. These levels are well below what is detected or reported for other product quality attributes. Subvisible particles remain a product quality attribute that is also qualified in clinical trials.
- 出版日期2010-8
